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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640113Generated: October 26, 2026

Sulfuric Acid → Methyl 7-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate

https://huagongshe.com/reaction/1640113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantMethyl 7-methoxy-1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 14722817—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
ProductMethyl 7-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 1305828471%

Reaction Steps

A slurry of methyl 7-methoxy-1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate (6.0 g, 26 mmol) and 10% palladium on carbon (100 mg) in AcOH (120 mL), and concentrated sulfuric acid (780 μL) was allowed to stir under 30 psi of hydrogen for 2.5 h. The reaction mixture was diluted with chloroform, and filtered through Celite. The filtrate was washed with water (5×), dried over Na2SO4 and evaporated. The residue was purified by filtration through a pad of silica, to give methyl 7-methoxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylate as an oil (4.03 g, 71%). 1H NMR (300 MHz, CD3OD): δ 6.94 (d, 1H), 6.67-6.62 (m, 2H), 3.72 (s, 3H), 3.69 (s, 3H), 2.94-2.91 (m, 2H), 2.78-2.70 (m, 3H), and 2.18-2.09 (m, 1H), and 1.86-1.73 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110687B2
Source datasetuspto-grants-2012_02
ORD IDord-0db14d2d357b47daa9112ca49aea7d90
Source noteuspto-grants-2012_02